Job TitlePrimary & Secondary Skill: SDTM/Clinical SAS1. Must have 6-8 years of experience in the clinical domain2. Strong knowledge of SDTM3.
Create advanced SAS macros, templates, and utilities for efficient data processing4. Act as the primary programming point of contact for biostatisticians and study teams5. Perform peer review of code and documentation for accuracy and traceability6.
Review CRF (Case Report Form) annotations and data specifications7. Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelinesSkill:1. Extensive programming experience in a clinical trial environment (CRO/Pharma)2.
Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO3. In-depth knowledge of CDISC standards and regulatory submission requirements